Technical Field
The present disclosure relates generally to the field of combustion furnaces and methods of use to produce glass, and more specifically to methods and systems to destabilize foam in glass handling equipment downstream of a submerged combustion melter.
Background Art
A submerged combustion melter (SCM) may be employed to melt glass batch materials to produce molten glass by passing oxygen, oxygen-enriched mixtures, or air along with a liquid, gaseous fuel, or particulate fuel in the glass batch, directly into a molten pool of glass usually through burners submerged in a glass melt pool. The introduction of high flow rates of oxidant and fuel into the molten glass, and the expansion of the gases cause rapid melting of the glass batch and much turbulence, and possibly foaming. Certain SCMs and/or flow channels may employ one or more high momentum burners, for example, to impinge on portions of a foam layer. High momentum burners are disclosed in Applicant's U.S. Pat. No. 9,021,838. “High momentum” combustion burners means burners configured to have a fuel velocity ranging from about 150 ft./second to about 1000 ft./second (about 46 meters/second to about 305 meters/second) and an oxidant velocity ranging from about 150 ft./second to about 1000 ft./second (about 46 meters/second to about 305 meters/second).
Often it is a primary goal to melt batch or other feed materials in an SCM as quickly and with as small a footprint SCM as possible. Although this is still desired for the most part, one drawback to this strategy in known submerged combustion systems and methods of melting glass-forming materials using an SCM is the tendency of the foam formed in the SCM to be resistant to destruction or even reduction. This may cause one or more problems in equipment downstream of the SCM, for example, glass conditioning and transport may be hindered as the foam layer may serve as an insulator and may limit the amount of energy capable of being transferred to the molten glass to maintain its temperature. Foam found in (or on top of) glasses typically exists as stable tetrahedral bubbles which need an outside influence to de-stabilize them and therefore break the foam, allowing heat transfer into the glass from burners located above the glass line. In addition, the foam may be destructive of forehearth heating systems and construction materials. In extreme cases, the foam may cause systems to require shutdown, maintenance and may result in a process upset. Attempts to reduce the foam through process adjustments, summarized in “Glass Industry of the Future”, U.S Dept. of Energy, Report 02-GA50113-03, Sep. 30, 2008, such as use of helium and steam to scavenge and consolidate bubbles, sonic methods to consolidate bubbles, vacuum to increase bubble size, and centrifugal force have not met with complete success in reducing foam to an acceptable amount.
It would be an advance in the glass manufacturing art if foam produced during submerged combustion melting of glass-forming materials could be de-stabilized, reduced, or even completely destroyed in equipment downstream of the SCM.
In accordance with the present disclosure, methods and systems are described which reduce or overcome one or more of the above problems.
A first aspect of the disclosure is a method comprising:
flowing a molten mass of glass and bubbles into an apparatus downstream of a submerged combustion melter, the downstream apparatus comprising a floor, a roof, and a wall connecting the floor and the roof, the downstream apparatus devoid of submerged combustion burners and other components that would increase turbulence of the molten mass, the molten mass having foam on at least a portion of a top surface of the molten mass; and
imposing a de-stabilizing force directly to the foam or to the molten mass and foam, the force selected from the group consisting of a vibratory force, an acoustic wave force, a particulate-based force, and a non-particulate-based mechanical force.
A second aspect of the disclosure is a system comprising:
an apparatus configured to be fluidly connected downstream of a submerged combustion melter, the downstream apparatus comprising a floor, a roof, a wall structure connecting the floor and roof, the floor, roof, and wall structure defining an internal space configured to contain a flowing or non-flowing molten mass of glass and foam, the apparatus devoid of submerged combustion burners and other components that would increase turbulence of the molten mass, the molten mass having foam on at least a portion of a top surface of the molten mass; and
one or more de-stabilization apparatus configured to impose a de-stabilizing force directly to the foam or to the molten mass and foam, the de-stabilization apparatus selected from the group consisting of a vibration apparatus, an acoustic wave force generating apparatus, a particulate-based force generating apparatus, and a non-particulate-based mechanical force generating apparatus.
Methods and systems of this disclosure will become more apparent upon review of the brief description of the drawings, the detailed description of the disclosure, and the claims that follow.
The manner in which the objectives of the disclosure and other desirable characteristics can be obtained is explained in the following description and attached drawings in which:
It is to be noted, however, that the appended drawings are not to scale and illustrate only typical embodiments of this disclosure, and are therefore not to be considered limiting of its scope, for the disclosure may admit to other equally effective embodiments.
In the following description, numerous details are set forth to provide an understanding of the disclosed systems and methods. However, it will be understood by those skilled in the art that the systems and methods covered by the claims may be practiced without these details and that numerous variations or modifications from the specifically described embodiments may be possible and are deemed within the claims. All U.S. published patent applications and U.S. patents referenced herein are hereby explicitly incorporated herein by reference. In the event definitions of terms in the referenced patents and applications conflict with how those terms are defined in the present application, the definitions for those terms that are provided in the present application shall be deemed controlling.
As explained briefly in the Background, one drawback to present submerged combustion melting systems and methods is that the foam formed in the SCM may cause one or more problems in equipment downstream of the SCM, for example, glass conditioning and transport may be hindered as the foam layer may serve as an insulator and may limit the amount of energy capable of being transferred to the molten glass to maintain its temperature. Foam found in (or on top of) glasses typically exists as stable tetrahedral bubbles which need an outside influence to de-stabilize them and therefore break the foam.
Applicants have discovered certain methods and systems that may reduce or eliminate such shortcomings.
Various terms are used throughout this disclosure. “Submerged” as used herein means that combustion gases emanate from a combustion burner exit that is under the level of the molten glass; and “non-submerged” means that combustion gases do not emanate from combustion burner exits under the level of molten glass. Both submerged and non-submerged burners may be roof-mounted, floor-mounted, wall-mounted, or any combination thereof (for example, two floor mounted burners and one wall mounted burner). “SC” as used herein means “submerged combustion” unless otherwise specifically noted, and “SCM” means submerged combustion melter unless otherwise specifically noted.
The terms “foam” and “foamy” include froths, spume, suds, heads, fluffs, fizzes, lathers, effervesces, layer and the like. The term “bubble” means a thin, shaped, gas-filled film of molten glass. The shape may be spherical, hemispherical, rectangular, polyhedral, ovoid, and the like. The gas or “bubble atmosphere” in the gas-filled SC bubbles may comprise oxygen or other oxidants, nitrogen, combustion products (including but not limited to, carbon dioxide, carbon monoxide, NOx, SOx, H2S, and water), reaction products of glass-forming ingredients (for example, but not limited to, sand (primarily SiO2), clay, limestone (primarily CaCO3), burnt dolomitic lime, borax and boric acid, and the like. Bubbles may include solids particles, for example soot particles, either in the film, the gas inside the film, or both.
As used herein the term “combustion” means deflagration-type combustion unless other types of combustion are specifically noted, such as detonation-type combustion. Deflagration is sub-sonic combustion that usually propagates through thermal conductivity; hot burning material heats the next layer of cold material and ignites it. Detonation is supersonic and primarily propagates through shock. As used herein the terms “combustion gases” and “combustion products” means substantially gaseous mixtures of combusted fuel, any excess oxidant, and combustion products, such as oxides of carbon (such as carbon monoxide, carbon dioxide), oxides of nitrogen, oxides of sulfur, and water, whether from deflagration, detonation, or combination thereof. Combustion products may include liquids and solids, for example soot and unburned or non-combusted fuels.
“Oxidant” as used herein includes air and gases having the same molar concentration of oxygen as air, oxygen-enriched air (air having oxygen concentration greater than 21 mole percent), and “pure” oxygen, such as industrial grade oxygen, food grade oxygen, and cryogenic oxygen. Oxygen-enriched air may have 50 mole percent or more oxygen, and in certain embodiments may be 90 mole percent or more oxygen.
The term “fuel”, according to this disclosure, means a combustible composition comprising a major portion of, for example, methane, natural gas, liquefied natural gas, propane, hydrogen, steam-reformed natural gas, atomized hydrocarbon oil, combustible powders and other flowable solids (for example coal powders, carbon black, soot, and the like), and the like. Fuels useful in the disclosure may comprise minor amounts of non-fuels therein, including oxidants, for purposes such as premixing the fuel with the oxidant, or atomizing liquid or particulate fuels. As used herein the term “fuel” includes gaseous fuels, liquid fuels, flowable solids, such as powdered carbon or particulate material, waste materials, slurries, and mixtures or other combinations thereof.
The sources of oxidant and fuel may be one or more conduits, pipelines, storage facility, cylinders, or, in embodiments where the oxidant is air, ambient air. Oxygen-enriched oxidants may be supplied from a pipeline, cylinder, storage facility, cryogenic air separation unit, membrane permeation separator, or adsorption unit such as a vacuum swing adsorption unit.
The term “downstream apparatus” means a container, channel or conduit defined at least by a floor and a wall structure extending upwards from the floor to form a space in which molten glass may be present, whether flowing or not. In certain embodiments the downstream apparatus will include a roof and a wall structure connecting the floor and roof. The downstream apparatus may have any operable cross-sectional shape (for example, but not limited to, rectangular, oval, circular, trapezoidal, hexagonal, and the like) and any flow path shape (for example, but not limited to, straight, zigzag, curved, and combinations thereof). In certain systems and methods the downstream apparatus may be a flow channel selected from the group consisting of a conditioning channel, a distribution channel, and a forehearth.
Conduits used in particle guns and other devices, such as hoppers used for delivery of particles, and mechanical structures such as screens, paddles, blades, and the like useful in systems and methods of the present disclosure may be comprised of metal, ceramic, ceramic-lined metal, or combination thereof. Suitable metals include stainless steels, for example, but not limited to, 306 and 316 steel, as well as titanium alloys, aluminum alloys, and the like. Suitable materials for the glass-contact refractory, which may be present in SC melters and flow channels, and refractory burner blocks (if used), include fused zirconia (ZrO2), fused cast AZS (alumina-zirconia-silica), rebonded AZS, or fused cast alumina (Al2O3). The particular system and method, downstream apparatus, burner geometry, foam de-stabilization apparatus, and type of glass to be produced may all dictate the choice of a particular material, among other parameters.
Certain foam de-stabilization apparatus useful in systems and methods of this disclosure may be fluid-cooled.
Certain systems of this disclosure may comprise one or more non-submerged detonation combustion burners, which may be used for heating and/or foam destruction purposes. Suitable non-submerged combustion burners may comprise a fuel inlet conduit having an exit nozzle, the conduit and nozzle inserted into a cavity of a ceramic burner block, the ceramic burner block in turn inserted into either the roof or the wall structure, or both the roof and wall structure of the downstream apparatus.
In certain systems, one or more detonation and deflagration combustion burners may be adjustable with respect to direction of flow of the combustion products. Adjustment may be via automatic, semi-automatic, or manual control. Certain system embodiments may comprise a burner mount that mounts the burner in the wall structure, roof, or floor of the downstream apparatus comprising a refractory, or refractory-lined ball joint. Other burner mounts may comprise rails mounted in slots in the wall or roof. In yet other embodiments the burners may be mounted outside of the downstream apparatus, on supports that allow adjustment of the combustion products flow direction. Useable supports include those comprising ball joints, cradles, rails, and the like.
In certain systems and methods of the present disclosure, the downstream apparatus may comprise a flow channel comprising a series of sections, and may comprise one or more skimmers and/or impingement (high momentum) burners, such as described in assignee's U.S. Pat. Nos. 9,021,838 and 8,707,739. Certain systems and methods of the present disclosure may utilize measurement and control schemes such as described in Applicant's co-pending application U.S. Ser. No. 13/493,219, filed Jun. 11, 2012, now U.S. Pat. No. 9,096,453, issued Aug. 4, 2015, and/or feed batch densification systems and methods as described in Applicant's co-pending application U.S. Ser. No. 13/540,704, filed Jul. 3, 2012. Certain systems and methods of the present disclosure may utilize devices for delivery of treating compositions such as disclosed in Applicant's U.S. Pat. No. 8,973,405.
Certain system and method embodiments of this disclosure may be controlled by one or more controllers. For example, detonation burner and/or pulsed detonation device combustion (flame) temperatures may be controlled by monitoring one or more parameters selected from velocity of the fuel, velocity of the primary oxidant, mass and/or volume flow rate of the fuel, mass and/or volume flow rate of the primary oxidant, energy content of the fuel, temperature of the fuel as it enters the burner, temperature of the primary oxidant as it enters the burner, temperature of the effluent, pressure of the primary oxidant entering the burner, humidity of the oxidant, burner geometry, combustion ratio, and combinations thereof. Certain systems and methods of this disclosure may also measure and/or monitor feed rate of batch or other feed materials, such as glass batch, cullet, mat or wound roving and treatment compositions, mass of feed, and use these measurements for control purposes. Exemplary systems and methods of the disclosure may comprise a controller which receives one or more input parameters selected from temperature of melt, composition of bubbles and/or foam, height of foam layer, and combinations thereof, and may employ a control algorithm to control combustion temperature, flow rate and/or composition of foam de-stabilization compositions, vibration or oscillation of components, movement of mechanical foam de-stabilization devices into and out of contact with foam, and other output parameters based on one or more of these input parameters.
Specific non-limiting system and method embodiments in accordance with the present disclosure will now be presented in conjunction with the attached drawing figures. The same numerals are used for the same or similar features in the various figures. In the views illustrated in the drawing figures, it will be understood in each case that the figures are schematic in nature, and certain conventional features may not be illustrated in all embodiments in order to illustrate more clearly the key features of each embodiment. The geometry of forehearth 4 or other downstream apparatus is illustrated generally the same in the various embodiments, but that of course is not necessary.
The system embodiments illustrated in
SC burners (not illustrated) in SCM 2 produce a turbulent melt comprising bubbles having a bubble atmosphere. In general the atmosphere of the bubbles is about the same from bubble to bubble, but that is not necessarily so. The bubbles form bubble layer 18. One or more burners in SCM 2 may be oxy/fuel burners. SCM 2 may receive numerous feeds through one or more inlet ports, and batch feeders maybe provided. Other feeds are possible, such as glass mat waste, wound roving, waste materials, and the like, such as disclosed in Applicant's U.S. Pat. No. 8,650,914.
In accordance with the present disclosure, de-stabilization apparatus may be selected from vibration apparatus, acoustic wave force generating apparatus, particulate-based force generating apparatus, and non-particulate-based mechanical force generating apparatus. Embodiment 100 illustrated schematically in
Another class of de-stabilizing apparatus are acoustic wave force generating apparatus, one example including one or more pulsed, non-foam-impinging, non-submerged combustion burners as illustrated in embodiment 200 of
Valves 36, 38 and appropriate valve controls (not illustrated) may be provided to pulse or oscillate flow of fuel and/or oxidant flowing to burners 112, 114, and 116 through conduits 32, 34, respectively. Lines “P” indicate pulses of combustion products produced by pulsing or oscillating oxidant and/or fuel valves 36, 38. The pulsing may be random or non-random, and may provide certain benefits, such as reduced NOx emissions. The principle and the various methods of implementation are broadly described in U.S. Pat. No. 4,846,665, U.S. Pat. No. 5,302,111, U.S. Pat. No. 5,522,721, and U.S. Publication No. 2006/0177785. The main idea is to pulse the flow of fuel and/or oxidant being supplied to at least one burner 112, 114, 116, to generate successive fuel-rich and fuel-lean zones in a flame. In certain embodiments, the flow rate of a main or primary oxidant may be controlled by a main oxidant flow rate control unit, and oscillating combustion may be generated by oscillating the fuel flow with an oscillating valve and combusting the oscillating fuel with the main oxidant adjacent the burner to produce combustion products. A post-combustion oxidant may also be injected into the combustion products, and the injection rate of the post-combustion oxidant may be controlled by a post-combustion oxidant flow rate control unit. The combustion products and the injected post-combustion oxidant may then be combusted. A rate of the fuel flow may be predetermined. A controller may be provided that may be operatively associated with the main oxidant flow rate control unit, the oscillating valve, and the post-combustion oxidant flow rate control unit. A value or values associated with one or more combustion parameters (including a rate of flow of the main oxidant, a rate of flow of the post-combustion oxidant, a frequency of the oscillating fuel flow, an amplitude of the oscillating fuel flow, a duty cycle of the oscillating fuel flow) nay be determined. The combustion parameter associated with the determined value or values may be adjusted. The determined value or values may be based upon the predetermined fuel flow rate. The determining step may be performed by the controller.
In embodiment 200, burners 112, 114, and 116 may be high- or low-momentum detonation combustion burners, and the combustion products or flames do not directly impinge or touch foam layer 18 to de-stabilize the foam, but rely on acoustic wave forces as described.
Another embodiment including one or more acoustic wave force generating apparatus is embodiment 300 illustrated schematically in
Yet another embodiment including one or more acoustic wave force generating apparatus is embodiment 400 illustrated schematically in
In accordance with the present disclosure, speaker drivers may be mounted into a rigid enclosure of metal, ceramic material, or ceramic-coated metal, and mounted in roof 10 or wall 12 of downstream apparatus 4. The enclosures isolate the acoustic energy from the front of the cone from that of the back of the cone. A horn (not illustrated) may be employed to increase efficiency and directionality. A front grille or other acoustically neutral screen (not illustrated) may be provided to protect the driver from physical damage. In operation, a signal is delivered to the voice coil by means of electrical wires or wireless communication from an amplifier, then through flexible tinsel wire to the moving coil. The current creates a magnetic field that causes the diaphragm to be alternately attracted to, and repelled by, the fixed magnet as the electrical signal varies. The resulting back-and-forth motion drives the air in front of the diaphragm, resulting in pressure differentials that travel away as sound waves, indicated at “AW” in
In certain embodiments, such as embodiment 400 illustrated in
Those skilled in this art will readily recognize after having read this disclosure that systems and methods comprising combinations of any two or more of the various embodiments described herein may be combined. For example, systems and methods where vibration, such as in embodiment 100, may also include one or more speaker drivers, as in embodiment 400.
In order to determine which of the many foam de-stabilization apparatus and techniques may work best for any given situation may take a small amount of experimentation, but the degree of experimentation is not considered to be extensive or undue. Basically, the molten mass of glass and foam is allowed to enter the downstream apparatus, and one or more of the foam de-stabilization techniques begun soon thereafter, and tuned to achieve the greatest de-stabilization effect on the foam. If the foam for some reason is so stable as to not be affected at all by the particular de-stabilization apparatus or method, it may simply be discontinued.
Another class or type of foam de-stabilization system and method is the use of a particulate-based force generating apparatus. Two embodiments, 500 and 600, are now discussed in relation to
The particles used in embodiments 500 and 600 may have any composition suitable to break foam bubbles and not have a substantial deleterious effect on the molten glass being produced. The hoppers and particle guns may be configured to drop or shoot particles selected from sulfur-containing compounds, glass cullet, ground glass, particles comprising a chemistry compatible with and integratable into the molten glass (such as one or more of the ingredients listed in Table 1 for producing E-glass, or other glasses), frozen carbon dioxide, solid organic matter, and combinations and mixtures of any two or more of these. In certain embodiments the particles may “pop” or expand suddenly upon impacting the glass foam, providing a secondary foam de-stabilization or foam destruction mechanism. An example of this might be when using carbon dioxide snow or pellets, which through sublimation turn directly from solid to gas. Useful particulate materials may include certain nano-materials, for example but not limited to nanosilicon particles, nanoclays, carbon nanotubes, carbon spherical morphologies such as buckminsterfullerene (C60, C70, and the like), and diamond may act to impart one or more high-stress locations in a bubble film, forming one or more inclusions, and therefore reduce bubble stability. Certain of the above-mentioned nano-materials (such as nanoclays), in specified quantities, may increase stability of foams. Finally, it has been found that certain treatment compositions may function to both increase and decrease stability of bubbles in foam 18, depending on the quantity added. For example, sodium sulfate may act as both a stabilizing and a de-stabilizing agent depending on the quantity added. At low levels (about 1 wt. percent or lower, as a percentage of an aqueous treating composition) this compound may act as a surfactant and may improve stability of the bubbles. However at higher levels (about 5 wt. percent or above) the reduction in surface tension may overcome the stabilizing action of the surfactant and cause bubble collapse.
Particle guns may be configured to propel the plurality of particles using processes selected from non-reactive compressed gas propulsion, propulsion based on gas expansion due to one or more chemical reactions, electromagnetic propulsion, and combinations thereof. It is contemplated that use of non-reactive compressed gas propulsion will be the least expensive method, however this may not be true in all embodiments, and may not produce the best results in terms of foam de-stabilization.
Yet another type of foam de-stabilization of the present disclosure utilizes one or more non-particulate-based mechanical force generating apparatus in the downstream apparatus. Certain embodiments of this type of device comprise one or more screen-like foam-disturbing devices comprising a material resistant to the molten glass and foam in the downstream apparatus. Screen-like foam-disturbing devices may be selected from the group consisting of one or more screens, one or more nonwoven materials, and one or more woven materials. One system embodiment 700 of this type is illustrated schematically in
Another non-particulate-based mechanical force generating apparatus one or more non-screen-like, foam-disturbing devices comprising a material or materials resistant to the molten glass and foam in the downstream apparatus, and configured to contact at least a portion of the foam in a continuous or intermittent fashion. Certain embodiments of this type of foam de-stabilization device may comprise one or more moveable elongate members that are substantially parallel to a level of the molten glass in the downstream apparatus. Other embodiments of this type of foam de-stabilization device may comprise one or more moveable elongate members that are all substantially perpendicular to the level of the molten glass in the downstream apparatus. Yet other embodiments of this type of foam de-stabilization device may comprise one or more moveable relatively flat or curved plates, blades, paddles, or wings. Combinations of these embodiments may be employed as well, such as illustrated schematically in system embodiment 800 of
An embodiment 900 of foam de-stabilization device comprising one or more moveable relatively flat or curved plates, blades, paddles, or wings is illustrated schematically in
Systems and methods of the present disclosure may be combined with other strategies for foam de-stabilization. Systems and methods of the present disclosure decrease bubble stability when used separately or in conjunction with one or more downstream methods. For example, adding nitrogen as a treating composition to the molten mass of glass and bubbles in the downstream apparatus may tend to make bubbles in foam 18 less stable when there is the presence of a high moisture atmosphere in the downstream apparatus. A high moisture atmosphere may exist in the downstream apparatus for example when one or more high momentum burners (whether oxy/fuel or not) are used as impingement burners in the downstream apparatus to impinge on foam 18. The use of one or more high momentum impingement burners (whether oxy/fuel or not) in a downstream flow channel is described in Applicant's U.S. Pat. No. 8,707,739.
Measuring effectiveness of the foam de-stabilization systems and methods described here may generally be made by taking samples of the molten mass of glass and counting bubbles and their size in the molten mass, or a solidified or partially solidified sample thereof, using the naked eye. Another naked eye measurement may simply be comparing an acceptable glass to a glass sample made using a system and method of the present disclosure, and making a naked eye comparison. Another method would be to simply observe the height of foam or bubbles within a channel or other downstream apparatus, using graduated marks on refractory materials to serve as a ruler, or use of known heights of construction materials for the sidewalls to access the height of the foam. More sophisticated methods and equipment may certainly be used, such as image analysis using computers to measure size, size distribution and quantity of bubbles (or other parameters) within a high-resolution photograph or micrograph of the material to be analyzed. For example, companies such as Glass Service market methods and equipment for such measurements. The glass melting method, as well as phenomena within the melt, may be continuously observed, recorded and evaluated using a high temperature observation furnace equipped with a special silica observation crucible. This equipment may be further coupled with image analysis equipment to provide easy manipulation of recorded data. For example, in a “melt test”, the objective is to evaluate the fining characteristics of differing batch compositions. The area of the recorded images occupied by inhomogeneities (bubbles), bubble size distribution, bubble number, as well as bubble growth rates vs. melting time, may be evaluated to provide comparison between individual batches. The records of the melting course may be provided in the form of video files, which may be displayed on a personal computer, handheld computer, or other viewer. Bubble growth rate, or shrinkage rate, or rate of disappearance measurements may be based on direct observation and recording of bubble sizes depending on time. It is possible to keep bubbles suspended in the melt for hours by the developed “shuttle” method.
In embodiments of the present disclosure, a reduction of 5 percent, or 10 percent, or 20 percent, or 30 percent or more of foam may be acceptable. In other embodiments, nothing short of complete or substantially complete foam or bubble removal will suffice, in other words 90 percent, or 95 percent, or 99 percent, or even 99.9 percent reduction in foam and bubbles.
The downstream apparatus 4 may include one or more bushings (not illustrated) for example when producing glass fiber (not illustrated). Downstream apparatus for use in systems and methods of the present disclosure may comprise a roof, floor and sidewall structure comprised of an outer metal shell, non-glass-contact brick or other refractory wall, and glass-contact refractory for those portions expected to be in contact with molten glass. Downstream apparatus may include several sections arranged in series, each section having a roof, floor, and sidewall structure connecting its roof and floor, and defining a flow channel for conditioning molten glass flowing there through. The sections may be divided by a series of skimmers, each extending generally substantially vertically downward a portion of a distance between the roof and floor of the channel, with a final skimmer positioned between a last channel section and a forehearth. The number of sections and the number of skimmers may each be more or less than two. The downstream apparatus may be rectangular as illustrated in the various figures, or may be a shape such as a generally U-shaped or V-shaped channel or trough of refractory material supported by a metallic superstructure.
The flow rate of the molten glass through downstream apparatus 4 (unless it is a holding container without flow) will depend on many factors, including the geometry and size of the SCM and downstream apparatus, temperature of the melt, viscosity of the melt, and like parameters, but in general the flow rate of molten glass may range from about 0.5 lb./min to about 5000 lbs./min or more (about 0.23 kg/min to about 2300 kg/min or more), or from about 10 lbs./min to about 500 lbs./min (from about 4.5 kg/min to about 227 kg/min), or from about 100 lbs./min to 300 lbs./min (from about 45 kg/min to about 136 kg/min).
Low momentum detonation combustion burners useful in systems and methods of this disclosure may include some of the features of those disclosed in Applicant's U.S. Pat. No. 9,021,838. For low momentum burners using natural gas as fuel, the burners may have a fuel firing rate ranging from about 0.4 to about 40 scfh (from about 11 L/hr. to about 1,120 L/hr.); an oxygen firing rate ranging from about 0.6 to about 100 scfh (from about 17 L/hr. to about 2,840 L/hr.); a combustion ratio ranging from about 1.5 to about 2.5; nozzle velocity ratio (ratio of velocity of fuel to oxygen at the fuel nozzle tip) ranging from about 0.5 to about 2.5; a fuel velocity ranging from about 6 ft./second to about 40 ft./second (about 2 meters/second to about 12 meters/second) and an oxidant velocity ranging from about 6 ft./second to about 40 ft./second (about 2 meters/second to about 12 meters/second).
Those of skill in this art will readily understand the need for, and be able to construct suitable fuel supply conduits and oxidant supply conduits, as well as respective flow control valves, threaded fittings, quick connect/disconnect fittings, hose fittings, and the like.
Submerged combustion melters may be fed a variety of feed materials. The initial raw material may include any material suitable for forming molten glass such as, for example, limestone, glass, sand, soda ash, feldspar and mixtures thereof. A glass composition for producing glass fibers known as “E-glass” typically includes 52-56% SiO2, 12-16% Al2O3, 0-0.8% Fe2O3, 16-25% CaO, 0-6% MgO, 0-10% B2O3, 0-2% Na2O+K2O, 0-1.5% TiO2 and 0-1% F2. Other glass compositions may be used, such as those described in Applicant's U.S. Publication Nos. 2007/0220922 and 2008/0276652. The initial raw material to provide these glass compositions can be calculated in known manner from the desired concentrations of glass components, molar masses of glass components, chemical formulas of batch components, and the molar masses of the batch components. Typical E-glass batches include those reproduced in Table 1, borrowed from U.S. Publication No. 2007/0220922. Notice that during glass melting, carbon dioxide (from lime) and water (borax) evaporate. The initial raw material can be provided in any form such as, for example, relatively small particles.
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SCMs may also be fed by one or more roll stands, which in turn supports one or more rolls of glass mat, as described in Applicant's U.S. Pat. No. 8,650,914, incorporated herein by reference. In certain embodiments powered nip rolls may include cutting knives or other cutting components to cut or chop the mat (or roving, in those embodiments processing roving) into smaller length pieces prior to entering melter 602. Also provided in certain embodiments may be a glass batch feeder. Glass batch feeders are well-known in this art and require no further explanation.
Downstream apparatus may include refractory fluid-cooled panels. Liquid-cooled panels may be used, having one or more conduits or tubing therein, supplied with liquid through one conduit, with another conduit discharging warmed liquid, routing heat transferred from inside the melter to the liquid away from the melter. Liquid-cooled panels may also include a thin refractory liner, which minimizes heat losses from the melter, but allows formation of a thin frozen glass shell to form on the surfaces and prevent any refractory wear and associated glass contamination. Other useful cooled panels include air-cooled panels, comprising a conduit that has a first, small diameter section, and a large diameter section. Warmed air transverses the conduits such that the conduit having the larger diameter accommodates expansion of the air as it is warmed. Air-cooled panels are described more fully in U.S. Pat. No. 6,244,197. In certain embodiments, the refractory fluid cooled-panels are cooled by a heat transfer fluid selected from the group consisting of gaseous, liquid, or combinations of gaseous and liquid compositions that functions or is capable of being modified to function as a heat transfer fluid. Gaseous heat transfer fluids may be selected from air, including ambient air and treated air (for air treated to remove moisture), inert inorganic gases, such as nitrogen, argon, and helium, inert organic gases such as fluoro-, chloro- and chlorofluorocarbons, including perfluorinated versions, such as tetrafluoromethane, and hexafluoroethane, and tetrafluoroethylene, and the like, and mixtures of inert gases with small portions of non-inert gases, such as hydrogen. Heat transfer liquids may be selected from inert liquids that may be organic, inorganic, or some combination thereof, for example, salt solutions, glycol solutions, oils and the like. Other possible heat transfer fluids include steam (if cooler than the oxygen manifold temperature), carbon dioxide, or mixtures thereof with nitrogen. Heat transfer fluids may be compositions comprising both gas and liquid phases, such as the higher chlorofluorocarbons.
Certain embodiments may comprise a method control scheme for the downstream apparatus. For example, as explained in the '914 patent, a master method controller may be configured to provide any number of control logics, including feedback control, feed-forward control, cascade control, and the like. The disclosure is not limited to a single master method controller, as any combination of controllers could be used. The term “control”, used as a transitive verb, means to verify or regulate by comparing with a standard or desired value. Control may be closed loop, feedback, feed-forward, cascade, model predictive, adaptive, heuristic and combinations thereof. The term “controller” means a device at least capable of accepting input from sensors and meters in real time or near-real time, and sending commands directly to one or more foam de-stabilization elements, and/or to local devices associated with foam de-stabilization elements able to accept commands. A controller may also be capable of accepting input from human operators; accessing databases, such as relational databases; sending data to and accessing data in databases, data warehouses or data marts; and sending information to and accepting input from a display device readable by a human. A controller may also interface with or have integrated therewith one or more software application modules, and may supervise interaction between databases and one or more software application modules. The controller may utilize Model Predictive Control (MPC) or other advanced multivariable control methods used in multiple input/multiple output (MIMO) systems. As mentioned previously, the methods of Applicant's U.S. Pat. No. 8,973,400, using the vibrations and oscillations of the melter itself, may prove useful predictive control inputs.
The downstream apparatus floors and sidewall structures may include a glass-contact refractory lining. The glass-contact lining may be 1 centimeter, 2 centimeters, 3 centimeters or more in thickness, however, greater thickness may entail more expense without resultant greater benefit. The refractory lining may be one or multiple layers. Glass-contact refractory used in downstream apparatus described herein may be cast concretes such as disclosed in U.S. Pat. No. 4,323,718. Two cast concrete layers are described in the '718 patent, the first being a hydraulically setting insulating composition (for example, that known under the trade designation CASTABLE BLOC-MIX-G, a product of Fleischmann Company, Frankfurt/Main, Federal Republic of Germany). This composition may be poured in a form of a wall section of desired thickness, for example a layer 5 cm thick, or 10 cm, or greater. This material is allowed to set, followed by a second layer of a hydraulically setting refractory casting composition (such as that known under the trade designation RAPID BLOCK RG 158, a product of Fleischmann company, Frankfurt/Main, Federal Republic of Germany) may be applied thereonto. Other suitable materials for the downstream apparatus, components that require resistance to high temperatures, such as particle guns, rotating blades and paddles, and refractory block burners (if used) are fused zirconia (ZrO2), fused cast AZS (alumina-zirconia-silica), rebonded AZS, or fused cast alumina (Al2O3). The choice of a particular material is dictated among other parameters by the geometry of the downstream apparatus and the foam de-stabilization equipment used, and the type of glass to be produced.
Those having ordinary skill in this art will appreciate that there are many possible variations of the systems and methods described herein, and will be able to devise alternatives and improvements to those described herein that are nevertheless considered to be within the claims.
This application is a division of U.S. patent application Ser. No. 13/644,104 filed Oct. 3, 2012, now U.S. Pat. No. 9,096,452, issued Aug. 4, 2015. This application may be related to the following United States non-provisional patent applications assigned to the Applicant of the present application which are all incorporated by reference herein: U.S. Ser. No. 13/458,211, filed Apr. 27, 2012, now U.S. Pat. No. 9,145,319, issued Sep. 29, 2015; Ser. No. 13/493,219, filed Jun. 11, 2012, now U.S. Pat. No. 9,096,453, issued Aug. 4, 2015; Ser. No. 13/644,058, filed Oct. 3, 2012, now U.S. Pat. No. 9,492,831, issued Nov. 15, 2016 and Ser. No. 13/633,979 filed Oct. 3, 2012. This application may be related to the following United States Patents assigned to the Applicant of the present application which are all incorporated by reference herein: U.S. Pat. Nos. 8,707,739; 8,707,740; 8,769,992; 8,875,544; 8,973,405; 8,991,215; 8,997,525; 9,021,838; and 9,032,760.
Number | Name | Date | Kind |
---|---|---|---|
1716433 | McKelvey et al. | Jun 1929 | A |
1989103 | McKelvey et al. | Jan 1935 | A |
2174533 | See et al. | Oct 1939 | A |
2118479 | McCaskey | Jan 1940 | A |
2269459 | Kleist | Jan 1942 | A |
2432942 | See et al. | Dec 1947 | A |
2455907 | Slayter | Jan 1948 | A |
2679749 | Poole | Jun 1954 | A |
2718096 | Henry et al. | Sep 1955 | A |
2773545 | Petersen | Dec 1956 | A |
2781756 | Kobe | Feb 1957 | A |
2878644 | Fenn | Mar 1959 | A |
2890166 | Heinze | Jun 1959 | A |
2902029 | Hill | Sep 1959 | A |
2981250 | Stewart | Apr 1961 | A |
3020165 | Davis | Feb 1962 | A |
3056283 | Tiede | Oct 1962 | A |
3073683 | Switzer et al. | Jan 1963 | A |
3084392 | Labino | Apr 1963 | A |
3088812 | Bitterlich et al. | May 1963 | A |
3104947 | Switzer et al. | Sep 1963 | A |
3160578 | Saxton et al. | Dec 1964 | A |
3165452 | Williams | Jan 1965 | A |
3170781 | Keefer | Feb 1965 | A |
3174820 | See et al. | Mar 1965 | A |
3215189 | Bauer | Nov 1965 | A |
3224855 | Plumat | Dec 1965 | A |
3237929 | Plumat et al. | Mar 1966 | A |
3241548 | See et al. | Mar 1966 | A |
3245769 | Eck et al. | Apr 1966 | A |
3248205 | Dolf et al. | Apr 1966 | A |
3260587 | Dolf et al. | Jul 1966 | A |
3268313 | Burgman et al. | Aug 1966 | A |
3285834 | Guerrieri et al. | Nov 1966 | A |
3294512 | Penberthy | Dec 1966 | A |
3325298 | Brown | Jun 1967 | A |
3385686 | Plumat et al. | May 1968 | A |
3402025 | Garrett et al. | Sep 1968 | A |
3407805 | Bougard | Oct 1968 | A |
3407862 | Mustian, Jr. | Oct 1968 | A |
3421873 | Burgman et al. | Jan 1969 | A |
3432399 | Schutt | Mar 1969 | A |
3445214 | Oremesher | May 1969 | A |
3498779 | Hathaway | Mar 1970 | A |
3499743 | Fanica et al. | Mar 1970 | A |
3510393 | Burgman et al. | May 1970 | A |
3519412 | Olink | Jul 1970 | A |
3525674 | Barnebey | Aug 1970 | A |
3533770 | Adler et al. | Oct 1970 | A |
3563683 | Hess | Feb 1971 | A |
3592151 | Webber | Jul 1971 | A |
3592623 | Shepherd | Jul 1971 | A |
3606825 | Johnson | Sep 1971 | A |
3617234 | Hawkins et al. | Nov 1971 | A |
3627504 | Johnson et al. | Dec 1971 | A |
3692017 | Glachant et al. | Sep 1972 | A |
3717139 | Guillet et al. | Feb 1973 | A |
3738792 | Feng | Jun 1973 | A |
3746527 | Knavish et al. | Jul 1973 | A |
3747588 | Booth | Jul 1973 | A |
3754879 | Phaneuf | Aug 1973 | A |
3756800 | Phaneuf | Sep 1973 | A |
3763915 | Perry et al. | Oct 1973 | A |
3764287 | Brocious | Oct 1973 | A |
3771988 | Starr | Nov 1973 | A |
3818893 | Kataoka et al. | Jun 1974 | A |
3835909 | Douglas et al. | Sep 1974 | A |
3840002 | Douglas et al. | Oct 1974 | A |
3856496 | Nesbitt et al. | Dec 1974 | A |
3885945 | Rees et al. | May 1975 | A |
3907585 | Francel et al. | Sep 1975 | A |
3913560 | Lazarre et al. | Oct 1975 | A |
3951635 | Rough | Apr 1976 | A |
3976464 | Wardlaw | Aug 1976 | A |
4001001 | Knavish et al. | Jan 1977 | A |
4004903 | Daman et al. | Jan 1977 | A |
4083711 | Jensen | Apr 1978 | A |
4110098 | Mattmuller | Aug 1978 | A |
4153438 | Stream | May 1979 | A |
4185982 | Schwenninger | Jan 1980 | A |
4203761 | Rose | May 1980 | A |
4205966 | Horikawa | Jun 1980 | A |
4226564 | Takahashi et al. | Oct 1980 | A |
4238226 | Sanzenbacher et al. | Dec 1980 | A |
4249927 | Fakuzaki et al. | Feb 1981 | A |
4270740 | Sanzenbacher et al. | Jun 1981 | A |
4282023 | Hammel et al. | Aug 1981 | A |
4303435 | Sleighter | Dec 1981 | A |
4309204 | Brooks | Jan 1982 | A |
4323718 | Buhring et al. | Apr 1982 | A |
4349376 | Dunn et al. | Sep 1982 | A |
4360373 | Pecoraro | Nov 1982 | A |
4397692 | Ramge et al. | Aug 1983 | A |
4398925 | Trinh et al. | Aug 1983 | A |
4406683 | Demarest | Sep 1983 | A |
4413882 | Bailey et al. | Nov 1983 | A |
4424071 | Steitz et al. | Jan 1984 | A |
4432780 | Propster et al. | Feb 1984 | A |
4488537 | Laurent | Dec 1984 | A |
4539034 | Hanneken | Sep 1985 | A |
4542106 | Sproull | Sep 1985 | A |
4545800 | Won et al. | Oct 1985 | A |
4549896 | Streicher et al. | Oct 1985 | A |
4626199 | Bounini | Dec 1986 | A |
4632687 | Kunkle et al. | Dec 1986 | A |
4634461 | Demarest, Jr. et al. | Jan 1987 | A |
4657586 | Masterson et al. | Apr 1987 | A |
4723708 | Berger et al. | Feb 1988 | A |
4735642 | Jensen et al. | Apr 1988 | A |
4738938 | Kunkle et al. | Apr 1988 | A |
4758259 | Jensen | Jul 1988 | A |
4798616 | Knavish et al. | Jan 1989 | A |
4814387 | Donat | Mar 1989 | A |
4816056 | Tsai et al. | Mar 1989 | A |
4877436 | Sheinkop | Oct 1989 | A |
4882736 | Pieper | Nov 1989 | A |
4886539 | Gerutti et al. | Dec 1989 | A |
4919700 | Pecoraro et al. | Apr 1990 | A |
4927886 | Backderf et al. | May 1990 | A |
4953376 | Merlone | Sep 1990 | A |
5011086 | Sonnleitner | Apr 1991 | A |
5032230 | Shepherd | Jul 1991 | A |
5052874 | Johanson | Oct 1991 | A |
5062789 | Gitman | Nov 1991 | A |
5097802 | Clawson | Mar 1992 | A |
5168109 | Backderf et al. | Dec 1992 | A |
5169424 | Grinnen et al. | Dec 1992 | A |
5199866 | Joshi et al. | Apr 1993 | A |
5204082 | Schendel | Apr 1993 | A |
5299929 | Yap | Apr 1994 | A |
5360171 | Yap | Nov 1994 | A |
5374595 | Dumbaugh et al. | Dec 1994 | A |
5405082 | Brown et al. | Apr 1995 | A |
5449286 | Snyder et al. | Sep 1995 | A |
5473885 | Hunter, Jr. et al. | Dec 1995 | A |
5483548 | Coble | Jan 1996 | A |
5490775 | Joshi et al. | Feb 1996 | A |
5522721 | Drogue et al. | Jun 1996 | A |
5545031 | Joshi et al. | Aug 1996 | A |
5575637 | Slavejkov et al. | Nov 1996 | A |
5606965 | Panz et al. | Mar 1997 | A |
5613994 | Muniz et al. | Mar 1997 | A |
5615668 | Panz et al. | Apr 1997 | A |
5636623 | Panz et al. | Jun 1997 | A |
5672827 | Jursich | Sep 1997 | A |
5713668 | Lunghofer et al. | Feb 1998 | A |
5718741 | Hull et al. | Feb 1998 | A |
5724901 | Guy et al. | Mar 1998 | A |
5736476 | Warzke et al. | Apr 1998 | A |
5743723 | Iatrides et al. | Apr 1998 | A |
5765964 | Calcote et al. | Jun 1998 | A |
5814121 | Travis | Sep 1998 | A |
5829962 | Drasek et al. | Nov 1998 | A |
5833447 | Bodelin et al. | Nov 1998 | A |
5849058 | Takeshita et al. | Dec 1998 | A |
5863195 | Feldermann | Jan 1999 | A |
5887978 | Lunghofer et al. | Mar 1999 | A |
5944864 | Hull et al. | Aug 1999 | A |
5954498 | Joshi et al. | Sep 1999 | A |
5975886 | Philippe | Nov 1999 | A |
5979191 | Jian | Nov 1999 | A |
5984667 | Philippe et al. | Nov 1999 | A |
5993203 | Koppang | Nov 1999 | A |
6029910 | Joshi et al. | Feb 2000 | A |
6036480 | Hughes et al. | Mar 2000 | A |
6039787 | Edlinger | Mar 2000 | A |
6045353 | VonDrasek et al. | Apr 2000 | A |
6068468 | Philippe et al. | May 2000 | A |
6071116 | Philippe et al. | Jun 2000 | A |
6074197 | Philippe | Jun 2000 | A |
6077072 | Marin et al. | Jun 2000 | A |
6085551 | Pieper et al. | Jul 2000 | A |
6109062 | Richards | Aug 2000 | A |
6113389 | Joshi et al. | Sep 2000 | A |
6116896 | Joshi et al. | Sep 2000 | A |
6123542 | Joshi et al. | Sep 2000 | A |
6126438 | Joshi et al. | Oct 2000 | A |
6154481 | Sorg et al. | Nov 2000 | A |
6156285 | Adams et al. | Dec 2000 | A |
6171100 | Joshi et al. | Jan 2001 | B1 |
6178777 | Chenoweth | Jan 2001 | B1 |
6183848 | Turner et al. | Feb 2001 | B1 |
6210151 | Joshi et al. | Apr 2001 | B1 |
6210703 | Novich | Apr 2001 | B1 |
6237369 | LeBlanc et al. | May 2001 | B1 |
6241514 | Joshi et al. | Jun 2001 | B1 |
6244197 | Coble | Jun 2001 | B1 |
6244857 | VonDrasek et al. | Jun 2001 | B1 |
6247315 | Marin et al. | Jun 2001 | B1 |
6250136 | Igreja | Jun 2001 | B1 |
6250916 | Philippe et al. | Jun 2001 | B1 |
6274164 | Novich | Aug 2001 | B1 |
6276924 | Joshi et al. | Aug 2001 | B1 |
6276928 | Joshi et al. | Aug 2001 | B1 |
6293277 | Panz et al. | Sep 2001 | B1 |
6314760 | Chenoweth | Nov 2001 | B1 |
6314896 | Marin et al. | Nov 2001 | B1 |
6318126 | Takei et al. | Nov 2001 | B1 |
6332339 | Kawaguchi et al. | Dec 2001 | B1 |
6338337 | Panz et al. | Jan 2002 | B1 |
6344747 | Lunghofer et al. | Feb 2002 | B1 |
6357264 | Richards | Mar 2002 | B1 |
6386271 | Kawamoto et al. | May 2002 | B1 |
6398547 | Joshi et al. | Jun 2002 | B1 |
6418755 | Chenoweth | Jul 2002 | B2 |
6422041 | Simpson et al. | Jul 2002 | B1 |
6454562 | Joshi et al. | Sep 2002 | B1 |
6460376 | Jeanvoine et al. | Oct 2002 | B1 |
6536238 | Kawaguchi et al. | Mar 2003 | B2 |
6536651 | Ezumi et al. | Mar 2003 | B2 |
6558606 | Kulkarni et al. | May 2003 | B1 |
6578779 | Dion | Jun 2003 | B2 |
6660106 | Babel et al. | Dec 2003 | B1 |
6694791 | Johnson et al. | Feb 2004 | B1 |
6701617 | Li et al. | Mar 2004 | B2 |
6705118 | Simpson et al. | Mar 2004 | B2 |
6708527 | Ibarlucea et al. | Mar 2004 | B1 |
6711942 | Getman et al. | Mar 2004 | B2 |
6715319 | Barrow et al. | Apr 2004 | B2 |
6722161 | LeBlanc | Apr 2004 | B2 |
6736129 | Sjith | May 2004 | B1 |
6739152 | Jeanvoine et al. | May 2004 | B2 |
6796147 | Borysowicz et al. | Sep 2004 | B2 |
6797351 | Kulkarni et al. | Sep 2004 | B2 |
6854290 | Hayes et al. | Feb 2005 | B2 |
6857999 | Jeanvoine | Feb 2005 | B2 |
6883349 | Jeanvoine | Apr 2005 | B1 |
6918256 | Gutmark et al. | Jul 2005 | B2 |
7027467 | Baev et al. | Apr 2006 | B2 |
7116888 | Aitken et al. | Oct 2006 | B1 |
7134300 | Hayes et al. | Nov 2006 | B2 |
7168395 | Engdahl | Jan 2007 | B2 |
7231788 | Karetta et al. | Jun 2007 | B2 |
7273583 | Rue et al. | Sep 2007 | B2 |
7330634 | Aitken et al. | Feb 2008 | B2 |
7383698 | Ichinose et al. | Jun 2008 | B2 |
7392668 | Adams et al. | Jul 2008 | B2 |
7428827 | Maugendre et al. | Sep 2008 | B2 |
7441686 | Odajima et al. | Oct 2008 | B2 |
7448231 | Jeanvoine et al. | Nov 2008 | B2 |
7454925 | DeAngelis et al. | Nov 2008 | B2 |
7509819 | Baker et al. | Mar 2009 | B2 |
7565819 | Jeanvoine et al. | Jul 2009 | B2 |
7578988 | Jacques et al. | Aug 2009 | B2 |
7581948 | Borders et al. | Sep 2009 | B2 |
7622677 | Barberree et al. | Nov 2009 | B2 |
7624595 | Jeanvoine et al. | Dec 2009 | B2 |
7748592 | Koga et al. | Jul 2010 | B2 |
7767606 | McGinnis et al. | Aug 2010 | B2 |
7778290 | Sacks et al. | Aug 2010 | B2 |
7781562 | Crawford et al. | Aug 2010 | B2 |
7802452 | Borders et al. | Sep 2010 | B2 |
7832365 | Hannum et al. | Nov 2010 | B2 |
7845314 | Smith | Dec 2010 | B2 |
7855267 | Crawford et al. | Dec 2010 | B2 |
8033254 | Hannum et al. | Oct 2011 | B2 |
8279899 | Kitabayashi | Oct 2012 | B2 |
8285411 | Hull et al. | Oct 2012 | B2 |
8650914 | Charbonneau | Feb 2014 | B2 |
8707739 | Huber et al. | Apr 2014 | B2 |
8707740 | Huber et al. | Apr 2014 | B2 |
8769992 | Huber | Jul 2014 | B2 |
8875544 | Charbonneau | Nov 2014 | B2 |
8973400 | Charbonneau et al. | Mar 2015 | B2 |
8973405 | Charbonneau et al. | Mar 2015 | B2 |
8991215 | Shock et al. | Mar 2015 | B2 |
8997525 | Shock et al. | Apr 2015 | B2 |
9021838 | Charbonneau et al. | May 2015 | B2 |
9032760 | Charbonneau et al. | May 2015 | B2 |
9096453 | Charbonneau | Aug 2015 | B2 |
20020086077 | Noller et al. | Jul 2002 | A1 |
20020134112 | Barrow et al. | Sep 2002 | A1 |
20020152770 | Becher et al. | Oct 2002 | A1 |
20020162358 | Jeanvoine et al. | Nov 2002 | A1 |
20020166343 | LeBlanc | Nov 2002 | A1 |
20030015000 | Hayes et al. | Jan 2003 | A1 |
20030029197 | Jeanvoine et al. | Feb 2003 | A1 |
20030037571 | Kobayashi et al. | Feb 2003 | A1 |
20040131988 | Baker et al. | Jul 2004 | A1 |
20040168474 | Jeanvoine et al. | Sep 2004 | A1 |
20040224833 | Jeanvoine et al. | Nov 2004 | A1 |
20050039491 | Maugendre et al. | Feb 2005 | A1 |
20050103323 | Engdal | May 2005 | A1 |
20050236747 | Rue et al. | Oct 2005 | A1 |
20060000239 | Jeanvoine et al. | Jan 2006 | A1 |
20060174655 | Kobayashi et al. | Aug 2006 | A1 |
20060233512 | Aitken et al. | Oct 2006 | A1 |
20060257097 | Aitken et al. | Nov 2006 | A1 |
20060287482 | Crawford et al. | Dec 2006 | A1 |
20060293494 | Crawford et al. | Dec 2006 | A1 |
20060293495 | Crawford et al. | Dec 2006 | A1 |
20070106054 | Crawford et al. | May 2007 | A1 |
20070122332 | Jacques et al. | May 2007 | A1 |
20070130994 | Boratav et al. | Jun 2007 | A1 |
20070212546 | Jeanvoine et al. | Sep 2007 | A1 |
20070220922 | Bauer et al. | Sep 2007 | A1 |
20080035078 | Li | Feb 2008 | A1 |
20080227615 | McGinnis et al. | Sep 2008 | A1 |
20080256981 | Jacques et al. | Oct 2008 | A1 |
20080276652 | Bauer et al. | Nov 2008 | A1 |
20080293857 | Crawford et al. | Nov 2008 | A1 |
20090042709 | Jeanvoine et al. | Feb 2009 | A1 |
20090220899 | Spangelo et al. | Sep 2009 | A1 |
20100064732 | Jeanvoine et al. | Mar 2010 | A1 |
20100087574 | Crawford et al. | Apr 2010 | A1 |
20100089383 | Cowles | Apr 2010 | A1 |
20100120979 | Crawford et al. | May 2010 | A1 |
20100143601 | Hawtof et al. | Jun 2010 | A1 |
20100227971 | Crawford et al. | Sep 2010 | A1 |
20100236323 | D'Angelico et al. | Sep 2010 | A1 |
20100300153 | Zhang et al. | Dec 2010 | A1 |
20100304314 | Rouchy et al. | Dec 2010 | A1 |
20100307196 | Richardson | Dec 2010 | A1 |
20100326137 | Rouchy et al. | Dec 2010 | A1 |
20110054091 | Crawford et al. | Mar 2011 | A1 |
20110061642 | Rouchy et al. | Mar 2011 | A1 |
20110088432 | Pumode et al. | Apr 2011 | A1 |
20110107670 | Galley et al. | May 2011 | A1 |
20110236846 | Rue et al. | Sep 2011 | A1 |
20110308280 | Huber | Dec 2011 | A1 |
20120077135 | Charbonneau | Mar 2012 | A1 |
20130086944 | Shock et al. | Apr 2013 | A1 |
20130086949 | Charbonneau | Apr 2013 | A1 |
20130086950 | Huber et al. | Apr 2013 | A1 |
20130086951 | Charbonneau et al. | Apr 2013 | A1 |
20130086952 | Charbonneau et al. | Apr 2013 | A1 |
20130279532 | Ohnstede et al. | Oct 2013 | A1 |
20130283861 | Mobley et al. | Oct 2013 | A1 |
20140090422 | Charbonneau et al. | Apr 2014 | A1 |
20140090423 | Charbonneau et al. | Apr 2014 | A1 |
Number | Date | Country |
---|---|---|
44 24 814 | Jan 1996 | DE |
100 29 983 | Sep 2003 | DE |
10 2005 033330 | Aug 2006 | DE |
0 181 248 | Oct 1989 | EP |
1 337 789 | Dec 2004 | EP |
2 133 315 | Dec 2009 | EP |
1 986 966 | Apr 2010 | EP |
1 667 934 | Feb 2011 | EP |
2 397 446 | Dec 2011 | EP |
2 433 911 | Mar 2012 | EP |
2 578 548 | Apr 2013 | EP |
2 740 860 | Sep 1997 | FR |
191301772 | Jan 1914 | GB |
191407633 | Jan 1914 | GB |
164073 | May 1921 | GB |
1449439 | Sep 1976 | GB |
1 514 317 | Jun 1978 | GB |
1208172 | Jul 1989 | IT |
2000 0050572 | May 2000 | KR |
114827 | Jul 1999 | RO |
9855411 | Dec 1998 | WO |
2008103291 | Aug 2008 | WO |
2009091558 | Jul 2009 | WO |
2010011701 | Jan 2010 | WO |
2010045196 | Apr 2010 | WO |
2012048790 | Apr 2012 | WO |
2012125665 | Sep 2012 | WO |
Entry |
---|
EP0181248 A1 Machine Translation, Google Patents, Aug. 2, 2016. |
“AccuTru Temperature Measurement,” AccuTru International Corporation, 2003. |
“Glass Melting Technology—A Technical and Economic Assessment,” 2004, U.S. Department of Energy, pp. 1-292. |
“Canty Process Technology” brochure, date unknown, copy received in Apr. 2012 at American Institute of Chemical Engineers, Spring Meeting, Houston, TX. |
Olabin, V.M. et al, “Submerged Combustion Furnace for Glass Melts,” Ceramic Engineering and Science Proceedings, Jan. 1, 1996, pp. 84-92, vol. 17—No. 2, American Ceramic Society Inc., US. |
Higley, BA, Glass Melter System Technologies for Vitrification of High-Sodium Content Low-Level, Radioactive, Liquid Wastes—Phase I: SBS Demonstration With Simulated Low-Level Waste—Final Test Report, Westinghouse Hanford Company, release date, 1995. |
Report for Treating Hanford LAW and WTP SW Simulants: Pilot Plant Mineralizing Flowsheet Apr. 2009, Department of Energy Environment Management Consolidated Business Center by THOR Treatment Technologies, LLC. |
“Glass Technologies—The Legacy of a Successful Public-Private Partnership”, 2007, U.S. Department of Energy, pp. 1-32. |
Rue, “Energy-Efficient Glass Melting—The Next Generation Melter”, Gas Technology Institute, Project No. 20621 Final Report (2008). |
“Glass Industry of the Future”, United States Department of Energy, report 02-GA50113-03, pp. 1-17, Sep. 30, 2008. |
Stevenson, “Foam Engineering: Fundamentals and Applications”, Chapter 16, pp. 336-389, John Wiiey & Sons (Mar. 13, 2012). |
Clare et al., “Density and Surface Tension of Borate Containing Silicate Melts”, Glass Technology—European Journal of Glass Science and Technology, Part A, pp. 59-62, vol. 44, No. 2, Apr. 1, 2003. |
Seward, T.P., “Modeling of Glass Making Processes for Improved Efficiency”, DE-FG07-96EE41262, Final Report, Mar. 31, 2003. |
Conradt et al, Foaming behavior on glass melts, Glastechniche Berichte 60 (1987) Nr. 6, S. 189-201 Abstract Fraunhofer ISC. |
Kim et al., “Foaming in Glass Melts Produced by Sodium Sulfate Decomposition under isothermal Conditions”Journal of the American Ceramic Society, 74(3), pp. 551-555, 1991. |
Kim et al., “Foaming in Glass Melts Produced by Sodium Sulfate Decomposition under Ramp Heating Conditions”, Journal of the American Ceramic Society, 75(11), pp. 2959-2963, 1992. |
Kim et al., “Effect of Furnace Atmosphere on E-glass Foaming”, Journal of Non-Crystalline Solids, 352(50/51), pp. 5287-5295, 2006. |
Van Limpt et al., “Modelling the evaporation of boron species. Part 1. Alkali-free borosilicate glass melts”, Glass Technology—European Journal of Glass Science and Technology, Part A, 52(3): pp. 77-87, 2011. |
Number | Date | Country | |
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20150315057 A1 | Nov 2015 | US |
Number | Date | Country | |
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Parent | 13644104 | Oct 2012 | US |
Child | 14752348 | US |